Immediate Implant Using an Inverted Co-Axis at 12º Versus a Conventional

Status Recruiting

Clinical Trial Summary

This study is a randomised controlled clinical trial. The patients will be included for the placement of immediate implants with immediate crown placement, to replace maxillary anterior teeth. Any significant differences between the Co-Axis implant and a conventional conical implant will be evaluated.

Clinical Trial Description

Introduction: It is commonly known that the placement of an immediate implant is a technique-sensitive procedure, as the implant should be placed in the palatal aspect for the perfect prosthetic emergence and profile. In order to supply this complexity, there is a novel macroimplant design involving an implant with a 12º angled platform. This angulation of the coronal part of the implant allows perfect emergence of the placement of post-extraction implants, since it is placed at the center of the socket, acquiring the best possible bone. In addition, thanks to the angled neck, prosthetic emergence is ideal, as it is corrected and emerges through the cingulate area, thus securing a perfect emergence profile. Objectives: Primary Outcomes: Evaluate the percentage of success and survival of the Inverted Co-Axis 12º Southern Implants versus the Internal Conical (Deep Tapered Conical) South Implants on a 1-2-1 follow-up. Secondary Outcomes: 1. To evaluate the primary stability of both implant systems through a coefficient stability if implants using the Penguin RFA; 2. To evaluate the horizontal and vertical marginal bone loss via a CBCT, 1 year after implant placement; 3. To evaluate the soft tissues via the Pink Esthetic Score (PES) 1 year post-op. Materials and Methods: Patients were randomly assigned in 2 groups of 15 patients, conical or inverta co-axis implants. Immediate implants in the aesthetic zone of the superior maxilar were placed with an immediate provisional crown restoration. In the same surgery, a connective tissue graft was performed. Only type I sockets according to the Elian Classification were eligible for this study. ;

Study Design

Related Conditions & MeSH terms

Dental Implant Failed

Clinical Trial Details

NCT number	NCT06059105
Study type	Interventional
Source	Universitat Internacional de Catalunya
Contact	Andrea Galve
Phone	+34659051487
Email	andreagalve@UIC.es
Status	Recruiting
Phase	N/A
Start date	March 15, 2022
Completion date	September 15, 2024

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Immediate Implant Using an Inverted Co-Axis at 12º Versus a Conventional Conical Implant

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms